Drug History: NICARDIPINE HYDROCHLORIDE

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DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

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Label and Approval History

Drug Name:	NICARDIPINE HYDROCHLORIDE
FDA Application No:	(ANDA) 074642
Active Ingredient(s):	NICARDIPINE HYDROCHLORIDE
Company:	MYLAN

Label History

Labels are not available on this site for NICARDIPINE HYDROCHLORIDE, (ANDA) 074642

Approval History

Action Date	Supplement Number	Approval Type	Letters, Reviews, Labels, Patient Package Insert
1/24/2002	003	Labeling
2/4/2000	002	Labeling
4/7/1998	001	Chemistry
7/18/1996	000	Approval

Therapeutic Equivalents

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